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Oral administration of Enterococcus faecalis FK-23 suppresses Th17 cell development and attenuates allergic airway responses in mice

机译:口服粪肠球菌FK-23可抑制Th17细胞发育并减弱小鼠的过敏性气道反应

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摘要

Evidence is increasing that oral administration of probiotics can attenuate asthmatic responses both in murine models and clinical trials. T-helper 17 (Th17) cells, a subset of CD4 + T cells have been implicated as having an important role in the development of several allergic disorders, but the relationship between oral administration of probiotics and Th17 development has not been well studied. BALB/c mice were given lysed Enterococcus faecalis FK-23 (LFK) orally for 28 days. After sensitization by subcutaneous injection of ovalbumin (OVA) on Days 14 and 21 and 1% OVA inhalation on Days 25, 26 and 27, they were challenged with a 5% OVA aerosol on Day 28. Twenty-four hours later, airway resistance and accumulation of inflammatory cells in bronchoalveolar lavage fluid (BALF) and lung tissues were determined. Interleukin (IL)-17-expressing CD4 + lymphocytes isolated from lung, spleen and lamina propria of the intestine were detected by flow cytometry. The expression of IL-6 and TGF-β mRNA was assessed by real-time PCR. Increases in airway hyperresponsiveness, and numbers of total leukocytes and mast cells in BALF induced by OVA challenge were significantly suppressed by oral administration of LFK. The increased percentage of IL-17-expressing CD4 + cells from lung, spleen and intestine in OVA-challenged mice was reduced following LFK treatment. We conclude that the oral administration of LFK suppresses the asthmatic response and that this is associated with attenuation of Th17 cell development.
机译:越来越多的证据表明,口服益生菌可以减轻小鼠模型和临床试验中的哮喘反应。 T-helper 17(Th17)细胞是CD4 + T细胞的一个子集,在几种过敏性疾病的发生中具有重要作用,但口服益生菌与Th17发育之间的关系尚未得到很好的研究。口服BALB / c小鼠粪便肠球菌FK-23(LFK)裂解28天。在第14和21天皮下注射卵清蛋白(OVA)致敏,并在第25、26和27天吸入1%OVA致敏后,在第28天用5%OVA气雾剂攻击他们。二十四小时后,呼吸道阻力和测定支气管肺泡灌洗液(BALF)和肺组织中炎性细胞的积累。通过流式细胞术检测从肠的肺,脾和固有层分离出的表达白介素(IL)-17的CD4 +淋巴细胞。通过实时PCR评估IL-6和TGF-βmRNA的表达。口服LFK可以显着抑制OVA激发引起的BALF中气道高反应性的增加和总白细胞和肥大细胞的数量。 LFK处理后,OVA攻击小鼠的肺,脾和肠中表达IL-17的CD4 +细胞百分比增加。我们得出结论,口服LFK可以抑制哮喘反应,这与Th17细胞发育的减弱有关。

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